Read more at http://www.littlemisshannah.org After 13 incredible years of serving Southern Nevada's rare disease community, our Little Miss Hannah Foundation will conclude its operations at the end of 2025. Started in memory of our beautiful and feisty daughter Hannah, LMHF has provided over 450 pieces of medical equipment, supporting over 500 local families, creating friendships and support networks that will last long beyond our foundation. After pouring our hearts into this mission, our family has decided it's time to step back and find a more personal way to honor Hannah's memory. Our equipment grant program will continue through August 2025, though it may end sooner if funds are depleted. We're so proud of the community you've built together - it's Hannah's true legacy. We are working with another organization to ensure our families can stay connected, and we'll share more details about this transition soon. Note: We are no longer accepting donations as we focus on serving our families through the remaining months. Our website will be updated in the coming weeks to reflect this change. From the bottom of our hearts, we thank our supporters, donors, families, friends, and the Las Vegas community for helping us make a difference in the lives of so many children with rare diseases and their families. (fb)

After 13 incredible years of serving Southern Nevada's rare disease community, our Little Miss Hannah Foundation will conclude its operations at the end of 2025. Started in memory of our beautiful and feisty daughter Hannah, LMHF has provided over 450 pieces of medical equipment, supporting over 500 local families, creating friendships and support networks that will last long beyond our foundation. After pouring our hearts into this mission, our family has decided it's time to step back and find a more personal way to honor Hannah's memory. Our equipment grant program will continue through August 2025, though it may end sooner if funds are depleted. We're so proud of the community you've built together - it's Hannah's true legacy. We are working with another organization to ensure our families can stay connected, and we'll share more details about this transition soon. Note: We are no longer accepting donations as we focus on serving our families through the remaining months. Our website will be updated in the coming weeks to reflect this change. From the bottom of our hearts, we thank our supporters, donors, families, friends, and the Las Vegas community for helping us make a difference in the lives of so many children with rare diseases and their families. (fb)